BEUDAMED
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    Dynamic Devices

    FDA registration
    Dynamic Devices·1 product·🇺🇸 United States

    Dynamic Device

    FDA UDI
    AVANTI ORTHOPAEDICS LLC·00810054091097·Dynamic Device

    DYNAMIC NEUROSCREENING DEVICE

    FDA 510(k)
    FDA Class 1 ·Neurology

    CANDELA DYNAMIC COOLING DEVICE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ANDELA DYNAMIC COOLING DEVICE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DYNAMIC COLLING DEVICE

    FDA Adverse Event
    Injury ·CANDELA CORP.·Product code GEH·June 12, 2002

    Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO VILLALBA·Product code DTB·May 21, 2026

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO VILLALBA·Product code DTB·May 21, 2026

    DEVICE #1 DMLC - DYNAMIC MULTILEAF COLLIMATOR

    FDA Adverse Event
    Malfunction ·3D LINE INTL.·Product code LXL·February 25, 2004

    WRIST ARTHRODESIS NAIL SYSTEM (IMPLATE)

    FDA Adverse Event
    Injury ·SKELETAL DYNAMICS·Product code HSB·October 1, 2014

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·December 3, 2024

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·July 11, 2025

    5.0MM TI LOCKING SCREW W/T25 STARDRIVE 30MM FOR IM NAILS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·March 26, 2014

    5.0MM TI LOCKING SCREW W/T25 STARDRIVE 42MM FOR IM NAILS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·March 26, 2014

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·November 6, 2024

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·May 20, 2024

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·March 6, 2025

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·March 30, 2026

    ALTIS SINGLE INCISION SLING SYSTEM

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code PAH·July 9, 2025